Canonical Allele Identifier: CA212183232

Gene: FGF8

Linked Data

• dbSNP Id: rs3218228
• gnomAD v4: 10-101775088-C-T
• MyVariant Identifiers: chr10:g.103534845C>T (hg19) ; chr10:g.101775088C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101775088C>T , CM000672.2:g.101775088C>T	GRCh38
NC_000010.10:g.103534845C>T , CM000672.1:g.103534845C>T	GRCh37
NC_000010.9:g.103524835C>T	NCBI36
NG_007151.1:g.5983G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000320185.7:c.156+42G>A MANE Select	ENSP00000321797.2:n.156+42G>A
ENST00000618991.5:c.-123-209G>A	ENSP00000484420.1:n.-123-209G>A
ENST00000344255.8:c.156+42G>A	ENSP00000340039.3:n.156+42G>A
ENST00000320185.6:c.156+42G>A	ENSP00000321797.2:n.156+42G>A
ENST00000344255.7:c.156+42G>A	ENSP00000340039.3:n.156+42G>A
ENST00000346714.7:c.70-209G>A	ENSP00000344306.3:n.70-209G>A
ENST00000347978.2:c.70-176G>A	ENSP00000321945.2:n.70-176G>A
ENST00000469792.6:c.*154-209G>A	ENSP00000473299.1:n.*154-209G>A
ENST00000485728.1:n.33-176G>A
ENST00000618991.4:c.-123-209G>A	ENSP00000484420.1:n.-123-209G>A
NM_001206389.1:c.-123-209G>A	NP_001193318.1:n.-123-209G>A
NM_006119.4:c.70-176G>A	NP_006110.1:n.70-176G>A
NM_033163.3:c.156+42G>A	NP_149353.1:n.156+42G>A
NM_033164.3:c.156+42G>A	NP_149354.1:n.156+42G>A
NM_033165.3:c.70-209G>A	NP_149355.1:n.70-209G>A
XM_011539509.1:c.79-176G>A	XP_011537811.1:n.79-176G>A
NM_006119.5:c.70-176G>A	NP_006110.1:n.70-176G>A
NM_033163.4:c.156+42G>A	NP_149353.1:n.156+42G>A
NM_033164.4:c.156+42G>A	NP_149354.1:n.156+42G>A
NM_033165.4:c.70-209G>A	NP_149355.1:n.70-209G>A
NM_001206389.2:c.-123-209G>A	NP_001193318.1:n.-123-209G>A
NM_006119.6:c.70-176G>A	NP_006110.1:n.70-176G>A
NM_033163.5:c.156+42G>A MANE Select	NP_149353.1:n.156+42G>A
NM_033165.5:c.70-209G>A	NP_149355.1:n.70-209G>A